Literature DB >> 25161206

Frontiers in nonclinical drug development: biosimilars.

A M Ryan1.   

Abstract

Biopharmaceuticals, produced by recombinant DNA technology, are generally more complicated to produce than small molecule drugs. As patents around the development and manufacturing of these biopharmaceuticals expire, biosimilars are being developed as comparable and more affordable alternatives to improve patient access and market competition. This commentary explains what a biosimilar is; it compares and contrasts biosimilar production with that of small molecule, generic, and other biological drugs; and it describes basic principles of the nonclinical development program for monoclonal antibody biosimilars.
© The Author(s) 2014.

Entities:  

Keywords:  biologics; biopharmaceuticals; biosimilar; drug development; monoclonal antibody; nonclinical; nonhuman primates; regulatory guidance

Mesh:

Substances:

Year:  2014        PMID: 25161206     DOI: 10.1177/0300985814547282

Source DB:  PubMed          Journal:  Vet Pathol        ISSN: 0300-9858            Impact factor:   2.221


  3 in total

Review 1.  The Role of Rituximab in Chronic Lymphocytic Leukemia Treatment and the Potential Utility of Biosimilars.

Authors:  Jennifer R Brown; Florence Cymbalista; Jeff Sharman; Ira Jacobs; Pilar Nava-Parada; Anthony Mato
Journal:  Oncologist       Date:  2017-12-06

2.  Biomedical and Market Issues Surrounding the Advent of Biosimilars.

Authors:  Abigail Cline; Jake E Turrentine
Journal:  Dermatol Ther (Heidelb)       Date:  2016-06-21

Review 3.  Pharmacovigilance of biosimilars - Why is it different from generics and innovator biologics?

Authors:  B Oza; S Radhakrishna; P Pipalava; V Jose
Journal:  J Postgrad Med       Date:  2019 Oct-Dec       Impact factor: 1.476

  3 in total

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